238 related articles for article (PubMed ID: 22544226)
1. HMGB1 gene knockout in mouse embryonic fibroblasts results in reduced telomerase activity and telomere dysfunction.
Polanská E; Dobšáková Z; Dvořáčková M; Fajkus J; Štros M
Chromosoma; 2012 Aug; 121(4):419-31. PubMed ID: 22544226
[TBL] [Abstract][Full Text] [Related]
2. HMGB2 is a negative regulator of telomerase activity in human embryonic stem and progenitor cells.
Kučírek M; Bagherpoor AJ; Jaroš J; Hampl A; Štros M
FASEB J; 2019 Dec; 33(12):14307-14324. PubMed ID: 31661640
[TBL] [Abstract][Full Text] [Related]
3. Nonhistone Proteins HMGB1 and HMGB2 Differentially Modulate the Response of Human Embryonic Stem Cells and the Progenitor Cells to the Anticancer Drug Etoposide.
Bagherpoor AJ; Kučírek M; Fedr R; Sani SA; Štros M
Biomolecules; 2020 Oct; 10(10):. PubMed ID: 33076532
[TBL] [Abstract][Full Text] [Related]
4. Expression of telomerase RNA template, but not telomerase reverse transcriptase, is limiting for telomere length maintenance in vivo.
Chiang YJ; Hemann MT; Hathcock KS; Tessarollo L; Feigenbaum L; Hahn WC; Hodes RJ
Mol Cell Biol; 2004 Aug; 24(16):7024-31. PubMed ID: 15282303
[TBL] [Abstract][Full Text] [Related]
5. Chromatin-associated proteins HMGB1/2 and PDIA3 trigger cellular response to chemotherapy-induced DNA damage.
Krynetskaia NF; Phadke MS; Jadhav SH; Krynetskiy EY
Mol Cancer Ther; 2009 Apr; 8(4):864-72. PubMed ID: 19372559
[TBL] [Abstract][Full Text] [Related]
6. Properties of Human Embryonic Stem Cells and Their Differentiated Derivatives Depend on Nonhistone DNA-Binding HMGB1 and HMGB2 Proteins.
Bagherpoor AJ; Dolezalova D; Barta T; Kučírek M; Sani SA; Ešner M; Kunova Bosakova M; Vinarský V; Peskova L; Hampl A; Štros M
Stem Cells Dev; 2017 Mar; 26(5):328-340. PubMed ID: 27863459
[TBL] [Abstract][Full Text] [Related]
7. ATR suppresses telomere fragility and recombination but is dispensable for elongation of short telomeres by telomerase.
McNees CJ; Tejera AM; Martínez P; Murga M; Mulero F; Fernandez-Capetillo O; Blasco MA
J Cell Biol; 2010 Mar; 188(5):639-52. PubMed ID: 20212315
[TBL] [Abstract][Full Text] [Related]
8. Telomerase variant A279T induces telomere dysfunction and inhibits non-canonical telomerase activity in esophageal carcinomas.
Zhang Y; Calado R; Rao M; Hong JA; Meeker AK; Dumitriu B; Atay S; McCormick PJ; Garfield SH; Wangsa D; Padilla-Nash HM; Burkett S; Zhang M; Kunst TF; Peterson NR; Xi S; Inchauste S; Altorki NK; Casson AG; Beer DG; Harris CC; Ried T; Young NS; Schrump DS
PLoS One; 2014; 9(7):e101010. PubMed ID: 24983628
[TBL] [Abstract][Full Text] [Related]
9. Short dysfunctional telomeres impair the repair of arsenite-induced oxidative damage in mouse cells.
Newman JP; Banerjee B; Fang W; Poonepalli A; Balakrishnan L; Low GK; Bhattacharjee RN; Akira S; Jayapal M; Melendez AJ; Baskar R; Lee HW; Hande MP
J Cell Physiol; 2008 Mar; 214(3):796-809. PubMed ID: 17849448
[TBL] [Abstract][Full Text] [Related]
10. Ku70 prevents genome instability resulting from heterozygosity of the telomerase RNA component in a vertebrate tumour line.
Faure V; Wenner T; Cooley C; Bourke E; Farr CJ; Takeda S; Morrison CG
DNA Repair (Amst); 2008 May; 7(5):713-24. PubMed ID: 18308646
[TBL] [Abstract][Full Text] [Related]
11. Stabilization of telomere length and karyotypic stability are directly correlated with the level of hTERT gene expression in primary fibroblasts.
Cui W; Aslam S; Fletcher J; Wylie D; Clinton M; Clark AJ
J Biol Chem; 2002 Oct; 277(41):38531-9. PubMed ID: 12122013
[TBL] [Abstract][Full Text] [Related]
12. Telomere maintenance requires the RAD51D recombination/repair protein.
Tarsounas M; Muñoz P; Claas A; Smiraldo PG; Pittman DL; Blasco MA; West SC
Cell; 2004 Apr; 117(3):337-47. PubMed ID: 15109494
[TBL] [Abstract][Full Text] [Related]
13. Phenotypes in mTERT⁺/⁻ and mTERT⁻/⁻ mice are due to short telomeres, not telomere-independent functions of telomerase reverse transcriptase.
Strong MA; Vidal-Cardenas SL; Karim B; Yu H; Guo N; Greider CW
Mol Cell Biol; 2011 Jun; 31(12):2369-79. PubMed ID: 21464209
[TBL] [Abstract][Full Text] [Related]
14. An intact putative mouse telomerase essential N-terminal domain is necessary for proper telomere maintenance.
Rousseau P; Khondaker S; Zhu S; Lauzon C; Mai S; Autexier C
Biol Cell; 2016 Apr; 108(4):96-112. PubMed ID: 26787169
[TBL] [Abstract][Full Text] [Related]
15. The telomerase activator TA-65 elongates short telomeres and increases health span of adult/old mice without increasing cancer incidence.
Bernardes de Jesus B; Schneeberger K; Vera E; Tejera A; Harley CB; Blasco MA
Aging Cell; 2011 Aug; 10(4):604-21. PubMed ID: 21426483
[TBL] [Abstract][Full Text] [Related]
16. Rescue of a telomere length defect of Nijmegen breakage syndrome cells requires NBS and telomerase catalytic subunit.
Ranganathan V; Heine WF; Ciccone DN; Rudolph KL; Wu X; Chang S; Hai H; Ahearn IM; Livingston DM; Resnick I; Rosen F; Seemanova E; Jarolim P; DePinho RA; Weaver DT
Curr Biol; 2001 Jun; 11(12):962-6. PubMed ID: 11448772
[TBL] [Abstract][Full Text] [Related]
17. Telomeric function of mammalian telomerases at short telomeres.
Fakhoury J; Marie-Egyptienne DT; Londoño-Vallejo JA; Autexier C
J Cell Sci; 2010 May; 123(Pt 10):1693-704. PubMed ID: 20427319
[TBL] [Abstract][Full Text] [Related]
18. Severe growth defect in mouse cells lacking the telomerase RNA component.
Niida H; Matsumoto T; Satoh H; Shiwa M; Tokutake Y; Furuichi Y; Shinkai Y
Nat Genet; 1998 Jun; 19(2):203-6. PubMed ID: 9620783
[TBL] [Abstract][Full Text] [Related]
19. Defective repair of oxidative base lesions by the DNA glycosylase Nth1 associates with multiple telomere defects.
Vallabhaneni H; O'Callaghan N; Sidorova J; Liu Y
PLoS Genet; 2013; 9(7):e1003639. PubMed ID: 23874233
[TBL] [Abstract][Full Text] [Related]
20. HMGB1 and HMGB2 cell-specifically down-regulate the p53- and p73-dependent sequence-specific transactivation from the human Bax gene promoter.
Stros M; Ozaki T; Bacikova A; Kageyama H; Nakagawara A
J Biol Chem; 2002 Mar; 277(9):7157-64. PubMed ID: 11748232
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
